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EMA Product

Prialt

Product approved by European Medicines Agency (EU)

Basic Information

Prialt

Regulatory Information

EMEA/H/C/000551

Authorised

February 21, 2005

November 18, 2004

31

June 21, 2024

Company Information

Germany

Hohenzollerndamm 150-151 14199 Berlin

Esteve Pharmaceuticals GmbH

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Ziconotide is indicated for the treatment of severe, chronic pain in patients who require intrathecal (IT) analgesia.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Prialt. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Prialt.

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